364 research outputs found

    Big bounce from spin and torsion

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    The Einstein-Cartan-Sciama-Kibble theory of gravity naturally extends general relativity to account for the intrinsic spin of matter. Spacetime torsion, generated by spin of Dirac fields, induces gravitational repulsion in fermionic matter at extremely high densities and prevents the formation of singularities. Accordingly, the big bang is replaced by a bounce that occurred when the energy density ϵgT4\epsilon\propto gT^4 was on the order of n2/mPl2n^2/m_\textrm{Pl}^2 (in natural units), where ngT3n\propto gT^3 is the fermion number density and gg is the number of thermal degrees of freedom. If the early Universe contained only the known standard-model particles (g100g\approx 100), then the energy density at the big bounce was about 15 times larger than the Planck energy. The minimum scale factor of the Universe (at the bounce) was about 103210^{32} times smaller than its present value, giving \approx 50 \mum. If more fermions existed in the early Universe, then the spin-torsion coupling causes a bounce at a lower energy and larger scale factor. Recent observations of high-energy photons from gamma-ray bursts indicate that spacetime may behave classically even at scales below the Planck length, supporting the classical spin-torsion mechanism of the big bounce. Such a classical bounce prevents the matter in the contracting Universe from reaching the conditions at which a quantum bounce could possibly occur.Comment: 6 pages; published versio

    Characterization of the n-TOF EAR-2 neutron beam

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    The experimental area 2 (EAR-2) at CERNs neutron time-of-flight facility (n-TOF), which is operational since 2014, is designed and built as a short-distance complement to the experimental area 1 (EAR-1). The Parallel Plate Avalanche Counter (PPAC) monitor experiment was performed to characterize the beam prole and the shape of the neutron 'ux at EAR-2. The prompt γ-flash which is used for calibrating the time-of-flight at EAR-1 is not seen by PPAC at EAR-2, shedding light on the physical origin of this γ-flash

    The measurement programme at the neutron time-of-flight facility n-TOF at CERN

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    Neutron-induced reaction cross sections are important for a wide variety of research fields ranging from the study of nuclear level densities, nucleosynthesis to applications of nuclear technology like design, and criticality and safety assessment of existing and future nuclear reactors, radiation dosimetry, medical applications, nuclear waste transmutation, accelerator-driven systems and fuel cycle investigations. Simulations and calculations of nuclear technology applications largely rely on evaluated nuclear data libraries. The evaluations in these libraries are based both on experimental data and theoretical models. CERN's neutron time-of-flight facility n-TOF has produced a considerable amount of experimental data since it has become fully operational with the start of its scientific measurement programme in 2001. While for a long period a single measurement station (EAR1) located at 185 m from the neutron production target was available, the construction of a second beam line at 20 m (EAR2) in 2014 has substantially increased the measurement capabilities of the facility. An outline of the experimental nuclear data activities at n-TOF will be presented

    Evaluation Of The Pharmacokinetic Interaction Between Candesartan Cilexetil And Felodipine

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    The study was performed to evaluate the pharmacokinetic interaction of test formulation of candesartan 16 mg tablet and felodipine extended release 5 mg tablet together in a combination package, comparing with the fasting period intake of commercial formulations of both Atacand® 16 mg tablet and Splendil® extended release 5 mg tablet (Test formulation and reference formulation from AstraZeneca, Brazil) in 36 volunteers of both sexes. The study was conducted open with randomized three period crossover design and a one week wash out period. The candesartan and felodipine were analyzed by LC-MS-MS. The mean ratio of parameters Cmax and AUC0-t and 90% confidence intervals of correspondents were calculated to determine the pharmacokinetic interaction. Geometric mean of candesartan exposure together in a combination package felodipine individual percent ratio was 102.51% AUC0-t and 110.40% for Cmax. The 90% confidence intervals were 90.00 - 116.77% and 93.94 - 129.74%, respectively. Geometric mean of felodipine exposure together in a combination package candesartan individual percent ratio was 102.69% AUC0-t and 96.17% for Cmax. The 90% confidence intervals were 89.46 - 117.88% and 82.07 - 112.69%, respectively. The major variable in this respect, AUC, was not signicantly affected by felodipine and candesartan with concomitant administration. The Cmax of candesartan was not signicantly affected by co-administration of felodipine. Based on these data and in presence in the market of isolated candersatana and felodipino formularizations used in combination in medical practice, it is concluded that there are no risk with concomitant administration between felodipine and candesartan.© 2011 Abib Jr E, et al.31510Blyckert, E., Wingstrand, K., Edgar, B., Lidman, K., Plasma concentration profiles® and antihypertensive effect of conventional and extended release felodipine tablets (1990) Br J Clin Pharmacol, 29, pp. 39-45Blychert, E., Edgar, B., Elmfeldt, D., Hedner, T., A population study of the pharmacokinetics of felodipine (1991) Blood Press, 31, pp. 15-24Blychert, E., Felodipine pharmacokinetics and plasma concentration vs effect relationships (1992) Blood Press, 2, pp. 1-30Dahlöf, B., Andersson, O.K., A felodipine-metoprolol extended-release tablet: Its properties and clinical development (1995) J Hum Hypertens, 9, pp. 43-47Dunselman, P.H., Edgar, B., Felodipine clinical pharmacokinetics (1991) Clin Pharmacokinet, 21, pp. 418-430Edgar, B., Regardh, C., Lundborg, G., Romare, P.S., Nyberg, G., Pharmacokinetics and pharmacodynamic studies of felodipine in healthy subjects after various single, oral and intravenous doses (1987) Biopharm. Drug Dispos, 8, pp. 235-248Eriksson, M., Nyberg, G., Lidman, K., Aiming for steady 24-hour plasma concentrations: A comparison of two calcium antagonist and beta-blocker combinations (1993) Blood Press Suppl, 1, pp. 16-21Gleiter, C.H., Morike, K.E., Clinical pharmacokinetics of candesartan (2002) Clin Pharmacokinet, 41, pp. 07-17Gradman, A.H., Lewin, A., Bowling, B.T., For the candesartan versus losartan efficacy comparison (CANDLE) study group. Comparative effects of candesartan cilexetil and losartan in patients with systemic hypertension (1999) Heart Dis, 1, pp. 52-57Hallin, L., Andren, L., Hansson, L., Controlled trial of nifedipine and bendroflumethiazide in hypertension (1983) J Cardiovasc Pharmacol, 5, pp. 1083-1085Hansson, L., Zanchetti, A., Carruthers, S.G., Effects of intensive bloodpressure lowering and low-dose aspirin in patients with hypertension: Principal results of the Hypertension Optimal Treatment (HOT) randomized trial (1998) Lancet, 351, pp. 1755-1762Hedner, T., Sjogren, E., Elmfeldt, D., Antihypertensive effects and pharmacokinetics of felodipine combined with a,-blocker and, a diuretic (1987) J Cardiovasc Pharmac, 10, pp. 177-184Ikechi, G.O., Brian, L.R., Update on the role of candesartan in the optimal management of hypertension and cardiovascular risk reduction (2010) Integrated Blood Pressure Control, 3, pp. 45-55Kloner, R.A., Weinberger, M., Pool, J.L., For the comparison of candesartan and amlodipine for safety, tolerability and efficacy (CASTLE) study investigators. Comparative effects of candesartan cilexetil and amlodipine in patients with mild systemic hypertension (2001) Am J Cardiol, 87, pp. 727-731Little, W.C., Cheng, C.P., Elvelin, L., Vascular selective calcium entry blockers in the treatment of cardiovascuolar disorders: Focus on felodipine. Cardiovasc (1995) Drugs Ther, 9, pp. 657-663Maccarthy, E.P., Dihydropyridines and beta-adrenoceptor antagonists as combination treatment in hypertension (1987) J Hypertens, 5, pp. 133-137Macconnachie, A.M., Maclean, D., Low dose combination antihypertensive therapy: Additional efficacy without additional adverse effects (1995) Drug Saf, 12, pp. 85-90Mann, S.J., Gerber, L.M., Low-dose alpha/beta blockade in the treatment of essential hypertension (2001) Am J Hypertens, 14, pp. 553-558Matheson, A.J., Cheer, S.M., Goa, K.L., Perindopril/indapamide 2/0.625 mg/ day: A review of its place in the management of hypertension (2001) Drugs, 61, pp. 1211-1229McFayden, R.J., Reid, J.L., Angiotensin receptor antagonists as a treatment for hypertension (1994) J Hypertens, 12, pp. 1333-1338Melian, E.B., Jarvis, B., Candesartan cilexetil plus hydrochlorothiazide combination: A review of its use in hypertension (2002) Drugs, 62, pp. 787-816Messerli, F.H., Combination therapy in hypertension (1992) J HumHypertens, 6, pp. 19-21Messerli, F.H., Chander, K., Cardiac effects of combination therapy in hypertension (2000) J Cardiovasc Pharmacol, 35, pp. 17-22Michalewicz, L., Messerli, F.H., Cardiac effects of calcium antagonists in systemic hypertension (1997) Am J Cardiol, 79, pp. 39-46Morgan, T., Anderson, A.A., Comparison of candesartan, felodipine, and their combination in the treatment of elderly patients with systolic hypertension (2002) Am J Hypertens, 15, pp. 544-549Morimoto, S., Ogibara, T., TCV-116: A new angiotensin n type-1 receptor antagonist (1994) Cardiovasc Drug Rev, 12, pp. 153-164Muller, J.E., Circadian variation in cardiovascular events (1999) AM J Hypertens, 12, pp. 35-42Nalbantgil, I., Önder, R., Kiliccioglu, B., Turkoglu, C., Combination therapy with verapamil and nitrendipine in patients with hypertension (1993) J Hum Hypertens, 7, pp. 305-308Nalbantgil, I., Önder, R., Nalbantgil, S., Sustained-release verapamil and trandolapril, alone and in combination, in the treatment of obese hypertensive patients: A double-blind pilot study (1996) Curr Ther Res Clin Exp, 57, pp. 990-997Nalbantgil, S., Nalbantgil, I., Önder, R., Clinically additive effect between doxazosin and amlodipine in the treatment of essential hypertension (2000) Am J Hypertens, 13, pp. 921-926Neutel, J.M., Low-dose antihypertensive combination therapy: Its rationale and role in cardiovascular risk management (1999) Am J Hypertens, 12, pp. 73-79Nishikawa, K., Naka, T., Chatani, F., Yoshimura, Y., Candesartan cilexetil: A review of its preclinical pharmacology (1997) J Human Hypertens, 11, pp. 9-17O'Brien, E.T., Mackinnon, J., Propranolol and polythiazide in the treatment of hypertension (1972) Br Heart J, 34, pp. 1042-1044Oparil, S., Levine, J.H., Zuschke, C.A., For the candesartan cilexetil study investigators. Effect of candesartan cilexetil in patients with severe systemic hypertension (1999) Am J Cardiol, 84, pp. 289-293Opie, L.H., Messerli, F.H., The choice of first-line therapy: Rationale for low-dose combinations of an angiotensin converting enzyme inhibitor and a diuretic (2001) J Hypertens Suppl, 19, pp. 17-21Philipp, T., Letzel, H., Arens, H.J., Dose-finding study of candesartan cilexetil plus hydrochlorothiazide in patients with mild to moderate hypertension (1997) J Hum Hypertens, 11, pp. 67-68Plouin, P.F., Combination therapy with candesartan cilexetil plus hydrochlorothiazide in patients unresponsive to low-dose hydrochlorothiazide (1997) J Hum Hypertens, 11, pp. 65-66Prichard, B.N., Combined alpha and beta receptor inhibition in the treatment of hypertension (1984) Drugs, 28, pp. 51-68Roca-Cusachs, A., Torres, F., Horas, M., Nitrendipine and enalapril combination therapy in mild to moderate hypertension: Assessment of doseresponse relationship by a clinical trial of factorial design (2001) J Cardiovasc Pharmacol, 38, pp. 840-849Saltiel, E., Ellrodt, A.G., Monk, J.P., A Review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hypertension (1988) Drugs, 36, pp. 387-428Sanem, N., Mehdi, Z., Filiz, O., Bahar, B., Istemi, N., Remzi, O., Mustafa, A., Comparison of candesartan and felodipine alone and combined in the treatment of hypertension: A single-center, double-blind, randomized, crossover trial (2003) Current Therapeutic Research, 64, pp. 380-388Schulman, D.S., Flores, A.R., Tugoen, J., Antihypertensive treatment in hypertensive patients with normal left ventricular remodeling and improved diastolic function (1996) Am J Cardiol, 78, pp. 56-60Sever, P.S., Poulter, N.R., Calcium antagonists and diuretics as combined therapy (1987) J Hypertens Suppl, 5, pp. 123-126Shibouta, Y., Pharmacological profile of a highly potent and long-acting angiotensin II receptor antagonist, 2-ethoxy-l-[[2'-(lH-tetrazol-5-yl]biphenyl-4-yl]methyl]- lH-benzimidazoie-7-carboxylic acid (CV-11974) and its prodrug, (+)-l-(cyciohexyioxycarbonyloxy)-ethyl-2-ethoxy-l-[[2'(lH-tetrazol5yl)biphenyl-4-yl]-methyl]-lH-benzimidazole-7-carboxylate (TCV-116] (1993) Pharmacol Exp Ther, 266, pp. 114-120Siegl, P.K.S., Kivlighn, S.D., Broten, T.P., Pharmacology of angiotensin II receptor antagonists: Comparison with renin inhibitors and angiotensinconverting enzyme inhibitors (1994) Expert Opin Invest Drugs, 3, pp. 925-944Sleight, P., Cardiac benefits of ACE inhibitors and calcium antagonists alone and in combination (1994) J Cardiovasc Pharmacol, 23, pp. 39-42Song, H., Bao, W., Wang, H., An, G., Feny, J., Wang, R., Zhang, Y., An, F., Effects of extended release felodipine on endothelial vasoactive substances in patients with essential hypertension (2008) Clin Chem Lab Med, 46, pp. 393-395Timmermans, P.B., Wong, P.C., Chiu, A.T., Angiotensin II receptors and angiotensin II receptor antagonists (1993) Pharmacol Rev, 45, pp. 205-251Walton, T., Symes, L.R., Felodipine and isradipine: New calcium-channelblocking agents for the treatment of hypertension (1993) Clin Pharm, 12, pp. 261-275Weir, M.R., The rationale for combination versus single-entity therapy in hypertension (1998) Am J Hypertens, 11, pp. 163-169Wingstrand, K., Abrahamsson, B., Edgar, B., Bioavailability from felodipine extended release tablets with deferent dissolution properties (1990) Int J Pharm, 60, pp. 151-156Yao, R., Cheng, X., Liao, Y.H., Molecular mechanisms of felodipine suppressing atheroscelerosis in high-cholesteroldiet apolipoprotein E-knockout mice (2008) J Cardiovasc Pharmacol, 51, pp. 188-195Yedinak, K.C., Lopez, L.M., Felodipine: A new dihydropyridine calcium channel antagonist (1991) DICP, 25, pp. 1193-120
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